Hokanson 03652
Hokanson 03652 is a Class II device made by D. E. Hokanson, Inc., listed in FDA GUDID since 9 Sep 2016 (UDI-DI 00817065020313), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00817065020313 | Date9 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00817065020313
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Hokanson
- Generic name
- Blood pressure cuff, reusable
- Model / Ref / Catalog
- 03652
- Primary DI / UDI-DI
- 00817065020313
- FDA product code
- DXQ
- GMDN term
- Blood pressure cuff, reusable
- Device class
- Class II
- Regulation number
- 870.1120
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 12 Centimeter
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